Cargando…
A patient with Camurati-Engelmann disease presenting bilateral TMJ ankylosis: A case report
Camurati-Engelmann Disease (CED), also known as progressive diaphyseal dysplasia, is a rare congenital disorder inherited in an autosomal-dominant pattern, most commonly affecting the skull and diaphysis of long tubular bones. Clinical symptoms start in early age and include ostealgia, muscle atroph...
Autores principales: | Salman, Nour J., Pimenta e Souza, Denis, Kuriki, Erika, Sant’Ana, Eduardo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452382/ https://www.ncbi.nlm.nih.gov/pubmed/32841778 http://dx.doi.org/10.1016/j.ijscr.2020.08.006 |
Ejemplares similares
-
Regarding Camurati-Engelmann Disease: To the Editor
por: Viana, Melissa Machado, et al.
Publicado: (2018) -
Regarding Camurati-Engelmann Disease: In Reply
por: Yuldashev, Alisher J., et al.
Publicado: (2018) -
Losartan improves clinical outcome in Camurati Engelmann Disease
por: Ayyavoo, Ahila, et al.
Publicado: (2013) -
Camurati-Engelmann Disease Association With Hypogonadism and Primary Hypothyroidism
por: Low, Soo Fin, et al.
Publicado: (2014) -
Camurati-Engelmann Disease with Good Treatment Response to Losartan
por: Abdulla, Mansoor Cherumkuzhiyil
Publicado: (2019)